IMZ BONE TACK SYSTEM— 510(k) K952167

Substantially Equivalent

Interpore Intl.

FDA 510(k) clearance K952167 for IMZ BONE TACK SYSTEM, Substantially Equivalent on 1995-11-21. Applicant: Interpore Intl..

Clearance details

Applicant: Interpore Intl.
Product code: Code DZL
Advisory panel: Dental
Date received: 1995-05-08
Decision date: 1995-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

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Adverse events under product code DZL

product code DZL

Injury: 168
Total: 168

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.